4.6 Article

Total Synthesis and Complete Structural Assignment of Gambieric Acid A, a Large Polycyclic Ether Marine Natural Product

Journal

CHEMICAL RECORD
Volume 14, Issue 4, Pages 678-703

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/tcr.201402052

Keywords

gambieric acids; marine dinoflagellates; natural products; polycyclic ethers; total synthesis

Funding

  1. Japan Society for the Promotion of Science (JSPS)
  2. Ministry of Education, Science, Sports, Culture and Technology, Japan (MEXT)
  3. ERATO Murata Lipid Active Structure Project from the Japan Science and Technology Agency (JST)
  4. Sumitomo Foundation
  5. Astellas Foundation for Research on Metabolic Disorders
  6. Banyu Life Science Foundation International
  7. Grants-in-Aid for Scientific Research [25282228, 23102016] Funding Source: KAKEN

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More than thirty years after the discovery of polycyclic ether marine natural products, they continue to receive intense attention from the chemical, biological, and pharmacological communities because of their potent biological activities and highly complex molecular architectures. Gambieric acids are intriguing polycyclic ethers that exhibit potent antifungal activity with minimal toxicity against mammals. Despite the recent advances in the synthesis of this class of natural products, gambieric acids remain unconquered due to their daunting structural complexity, which poses a formidable synthetic challenge to organic chemists. This paper reviews our long-term studies on the total synthesis, complete configurational reassignment, and structure-activity relationships of gambieric acid A over the last decade.

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